Yaya Mahmout
Institut national des sciences appliquées
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Yaya Mahmout.
Phytochemistry | 1995
René Dolmazon; Michel Albrand; Jean-Marie Bessière; Yaya Mahmout; Dorota Wernerowska; Krzysztof Kolodziejczyk
Abstract 16-Hydroxy-manoyloxide, a new derivative of manoyloxide, ambreinolide and norambreinolide have been isolated from the ethyl acetate extract of Kyllinga erecta rhizomes.
Phytochemistry | 1993
Yaya Mahmout; Jean-Marie Bessière; René Dolmazon
Abstract The structures of two diterpenoids, isolated from the rhizomes of Kyllinga erecta have been elucidated as 1β-hydroxymanoyloxide and 11α-hydroxy
Journal of Essential Oil Research | 2002
Yaya Mahmout; Jean-Marie Bessière; R. Dolmazon
Abstract The essential oil of the rhizomes of Cyperus maculatus Boëck was analyzed by GC and GC/MS. Forty components were identified, of which the major component was found to be mustakone (22%).
Flavour and Fragrance Journal | 2001
René Dolmazon; Yaya Mahmout; Jean-Marie Bessière
The structure of a diterpenoid isolated from the methylene chloride extract of Kyllinga erecta rhizomes has been elucidated as 11α-hydroxy-13-epi-manoyloxide by spectral analysis (1H, 13C and MS). Deoxygenation of this compound gave the well known 13-epi-manoyloxide. Copyright
African Journal of Biotechnology | 2012
Mahamat Nour Adam Sakine; Yaya Mahmout; M. G. Dijoux-Franca; Joachim Gbenou; Mansourou Moudachirou
Glucocapparin (I) used in this study was isolated from the seeds of Boscia senegalensis (family Capparidaceae). The structure of (I) was determined on the basis of an extensive analysis of the spectroscopic data. Brine shrimp lethality bioassay of (I) showed a marked significant cytotoxic activity with LC 50 = 16.482 �g/ml. Compound (I) reduced the liberation of glucose from the liver of rabbits. The active concentration was 30 mg/ml showing that the in vitro anti-hyperglycaemic effect shown could be related to the traditional use of B. senegalensis seeds in Chad against type 2 diabetes.
Journal of Essential Oil Research | 1996
Yves Pélissier; Anglade Malan; Yaya Mahmout; Jean-Marie Bessière
ABSTRACT The volatile concentrates of the fruits of Landolphia senegalensis (DC.) Kotschy et Peyr. and L. heudelotii DC. were analyzed by GC and GC/MS. More than 90% of the volatiles of L. senegalensis were identified, with linalool (18.0%) and α-terpineol (29.8%) being the major constituents, whereas more than 70% of the volatiles of L. heudelotii were characterized. The major constituents in the volatile concentrate of this latter species were linalool (10.5%) and (E)-β-farnesene (8.8%).
Journal of Agricultural and Food Chemistry | 1993
Yaya Mahmout; Jean Marie. Bessiere; René Dolmazon
African Journal of Biotechnology | 2010
Gouollaly Tsiba; Loumpangou Célestine Nkounkou; Yaya Mahmout; Jean Maurille Ouamba; Ange Antoine Abena; Jean-Claude Chalchat; Gilles Figueredo
African Journal of Biotechnology | 2005
Mbailao Mbaiguinam; Yaya Mahmout; Mianpereum Tarkodjiel; Bernard Delobel; Jean-Marie Bessière
Bulletin of The Chemical Society of Ethiopia | 2001
Yaya Mahmout; Jean Marie. Bessiere; René Dolmazon